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122839-51-4

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122839-51-4 Usage

General Description

2-Fluoro-D-phenylalanine is a chemically synthesized biochemical substance often used in scientific research. It is one of the variants of phenylalanine, an alpha-amino acid that's used in the biosynthesis of proteins, modified by the addition of a fluorine atom to the molecular structure. This fluorine substitution can change the behavior of the molecule, which makes 2-fluoro-D-phenylalanine useful in various medical and biochemical research, particularly in the studies related to amino acid metabolism and protein synthesis, as well as in the development of potential therapeutic drugs. This chemical should be handled with care due to its potential for harmful effects.

Check Digit Verification of cas no

The CAS Registry Mumber 122839-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,8,3 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 122839-51:
(8*1)+(7*2)+(6*2)+(5*8)+(4*3)+(3*9)+(2*5)+(1*1)=124
124 % 10 = 4
So 122839-51-4 is a valid CAS Registry Number.

122839-51-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-FLUORO-D-PHENYLALANINE

1.2 Other means of identification

Product number -
Other names H-D-Phe(2-F)-OH.HCl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:122839-51-4 SDS

122839-51-4Downstream Products

122839-51-4Relevant articles and documents

UNUSUAL AMINO ACIDS II. Asymmetric Synthesis of Fluorine Containing Phenylalanines

Krause, Hans-Walter,Kreuzfeld, Hans-Joern,Doebler, Christian,Taudien, Stefan

, p. 555 - 566 (2007/10/02)

Few (Z)-α-N-benzoylamino-β-(fluorophenyl)-acrylic acids and their esters were prepared by known procedures and hydrogenated to the corresponding optically active α-benzoyl-β-(fluorophenyl)-alanine derivatives with optical yields up to 90percent using the

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